Graft-modified ultrahigh-molecular-weight polyacrylamide and preparation method thereof
An ultra-high molecular weight, polyacrylamide technology, used in chemical instruments and methods, drilling compositions, etc., can solve problems such as poor oil displacement efficiency in temperature resistance, salt resistance and aging resistance, and achieve improved oil resistance. Effects of temperature and salt resistance, enhanced oil recovery, and increased three-dimensional network structure
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Embodiment 1
[0028] Inject 0.15mol of sodium p-chlorophenolate and 7.8mol of ethylene oxide into the dry reaction bottle, and after reacting at 58°C for 8 hours, add 0.15mol of 2,2,6,6-tetramethyl-4-epoxypropyl Oxypiperidine-1-oxyl radical, continue to react at 80°C for 5 hours, add isopropanol to terminate the reaction, and precipitate with ether to obtain polyethylene oxide with a molecular weight of 2200 in the hydrophilic segment X -PEO-NO·. Add 0.10 mol of the functionalized polymer prepared above, 2.0 mol of styrene (St), and 0.10 mol of benzoyl peroxide into the reactor, pass nitrogen to remove oxygen, stir and mix evenly, and react at 100°C for 6 hours. A block copolymer with a hydrophobic segment molecular weight of 2000 was obtained X -PEO- b -PS. 0.10 g of the obtained copolymer and 2.55 g of ultra-high molecular weight polyacrylamide with a viscosity-average molecular weight of 28 million were dispersed in 95 g of aqueous sodium bicarbonate solution (pH=7.8) under strong sti...
Embodiment 2
[0034] Inject 0.15mol of sodium o-bromophenolate and 6.0mol of ethylene oxide into the dry reaction bottle, and after reacting at 55°C for 8 hours, add 0.15mol of 2,2,6,6-tetramethyl-4-epoxypropyl Oxypiperidine-1-oxyl radical, continue to react at 82°C for 5 hours, add isopropanol to terminate the reaction, and precipitate with ether to obtain polyethylene oxide with a molecular weight of 1600 in the hydrophilic segment X -PEO-NO·. Add 0.10mol and 1.5mol of p-methylstyrene (MSt) and 0.10mol of tert-butyl peroxide 2-ethylhexanoate to the reactor, pass nitrogen to remove oxygen, stir and mix well , reacted at 102°C for 6 hours to obtain a block copolymer with a molecular weight of 1700 in the hydrophobic segment X -PEO- b -PMS. 0.12 g of the obtained copolymer and 3.02 g of ultra-high molecular weight polyacrylamide with a viscosity-average molecular weight of 28 million were dispersed in 99 g of sodium bicarbonate aqueous solution (pH=9.6) under the action of strong stirring...
Embodiment 3
[0037] Inject 0.13mol sodium m-bromophenolate and 3.8mol propylene oxide into the dry reaction flask, and after reacting at 50°C for 10 hours, add 0.135mol 2,2,6,6-tetramethyl-4-epoxypropyloxy Piperidine-1-oxyl free radicals, continue to react at 80°C for 5 hours, add isopropanol to terminate the reaction, and precipitate with ether to obtain polyoxypropylene with a molecular weight of 1650 in the hydrophilic segment X -PPO-NO·. Add 0.10 mol of the functionalized polymer prepared above, 1.6 mol of styrene (St), and 0.11 mol of benzoyl peroxide into the reactor, pass nitrogen to remove oxygen, stir and mix evenly, and react at 110°C for 5 hours. A block copolymer with a molecular weight of 1600 in the hydrophobic segment was obtained X -PPO- b -PS. 0.15 g of the obtained copolymer and 4.02 g of ultra-high molecular weight polyacrylamide with a viscosity-average molecular weight of 32 million were dispersed in 102 g of aqueous sodium hydroxide solution (pH=8.5) under strong s...
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